The Recall Desk

Hazard

Crush Injury recalls

87 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
87
Critical
11
Severe
24
Most recent
2026-06-18

Of the 87 crush injury recalls we have scored against our rubric, 11 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 24 (28%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all crush injury recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

51–75 of 87

  • HighNHTSA·16V644000·2016-09-06

    Mazda Recalls Vehicles Due to Corroded Lift Gate Support Struts

    Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.

    Product
    MAZDA — MAZDA MAZDASPEED3, MAZDA3, MAZDA5, CX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V473000·2015-07-28

    Altec Recalls 2006-2015 Aerial Devices Due to Outrigger Interlock Defect

    Altec Industries is recalling 2,514 aerial devices from 2006-2015 because the outrigger interlock system may fail to detect proper deployment, risking boom instability and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1377-2015·2015-04-15

    Carestream CS 8100 X-ray Device Recalled for Unexpected Head Descent

    Carestream Health is recalling CS 8100 panoramic X-ray units because the device head may descend unexpectedly. Approximately 3,110 units were distributed worldwide.

    Product
    CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic digital panoramic X-ray images to be used at the direction of healthcare professionals of the dento-maxillo-facial region of the human anatomy as diagnostic support
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1378-2015·2015-04-15

    Carestream CS 8100 3D Dental X-Ray Devices Recalled for Unexpected Head Descent

    Carestream Health is recalling 470 CS 8100 3D dental X-ray units because the device head may descend unexpectedly, posing a risk of injury to patients or operators.

    Product
    CS 8100 3D, CATALOG # (s): 5311162, 5311188. Intended to produce complete or segmented tomographic digital panoramic X-ray images and three-dimensional digital X-ray images of the dentomaxillo-facial area to be used at the direction of healthcare professionals as diagnostic su
    Category
    Medical Device
    Distribution
    46 states
  • HighNHTSA·15V200000·2015-04-03

    Audi Recalls 2015 Q3 Vehicles Due to Sunroof Safety Defect

    Volkswagen Group of America is recalling 3,646 2015 Audi Q3 vehicles because the sunroof may continue closing after the vehicle is turned off, posing an injury risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0896-2015·2015-01-07

    Hansen Medical Recalls Sensei X Robotic Catheter Systems Due to Loose Clamp

    Hansen Medical is recalling Sensei X Robotic Catheter Systems because a mechanical clamp may become loose, causing the device to fall and potentially injure patients or users.

    Product
    Sensei X Robotic Catheter System, model numbers 02057 and 08257. - Set up joint (SUJ)mechanical clamp that secures the SUJ to the catheter laboratory table. Product Usage: The Sensei X Robotic Catheter System is an electromechanical software controlled system designed to f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2709-2014·2014-10-01

    Philips Brilliance CT System Recalled for Finger Squeeze Hazard

    Philips is recalling 364 Brilliance CT systems due to a gap in the tilt stand covers that can squeeze fingers during gantry movement.

    Product
    Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Computed tomography scanner intended to provide cross sectional images of the human body and visualization of the internal organs.
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2137-2014·2014-08-13

    Carestream KODAK DirectView DR 9000 X-Ray System Recalled for Control Failure

    Carestream Health is recalling KODAK DirectView DR 9000 systems because a control failure may cause the U-Arm to move downward unexpectedly at three times the normal speed.

    Product
    KODAK DirectView DR 9000 System, Catalog Numbers 1966688 (US and Canada) and 8161937 (outside the US and Canada) --- A permanently installed diagnostic x-ray system composed of 3 main components: an operator console, U-Arm assembly with x-ray tube including a collimator, and a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1827-2014·2014-06-25

    Philips MR Trolley Recall for Foot Clamping Hazard

    Philips is recalling Height Adjustable FlexTrak trolleys and Trolley Variable Height IRFs for Ingenia MR systems due to a risk of foot clamping.

    Product
    Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T & 3.0T products) Product Usage: Diagnostic MR System. The Height Adjustable FlexTrak trolley and Trolley Variable Height IRF is an optional device designed to prepare the patient outside the examination room to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1826-2014·2014-06-25

    Philips Ingenia FlexTrak Trolley Recalled for Foot Clamping Hazard

    Philips is recalling Ingenia HA FLEX TRAK Trolleys because the central column can clamp a patient's foot. The recall covers 420 units distributed worldwide.

    Product
    Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia 1.5T & 3.0T products) Product Usage: Diagnostic MR System. The Height Adjustable FlexTrak trolley and Trolley Variable Height IRF is an optional device designed to prepare the patient outside the examination room t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1714-2014·2014-06-11

    Toshiba Infinix X-Ray System Recalled for Table Movement Safety Issue

    Toshiba is recalling two Infinix X-Ray Interventional Systems because the table may continue moving during longitudinal tilt despite error signals.

    Product
    Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1795-2013·2013-07-31

    Siemens Axiom Aristos MX Flat Panel Imager Recalled for Finger Injury Risk

    Siemens is recalling 401 Axiom Aristos MX digital imagers because the table top float function can trap and crush fingers.

    Product
    Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003. The device is used for diagnostic X-ray imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V346000·2012-07-19

    Collins Recalls 2012 School Buses Due to Door Entanglement Hazard

    Collins is recalling 171 model year 2012 school buses because clothing or backpack drawstrings can get caught in the open door, potentially pulling passengers under the vehicle.

    Product
    CORBEIL — CORBEIL, COLLINS, MID-BUS DE, SL, DH, SH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V191000·2012-05-02

    Chrysler and Dodge Recall 2012 Minivans for Liftgate Pinch Sensor Defect

    Chrysler is recalling 2012 Town and Country and Dodge Grand Caravan minivans because a faulty liftgate sensor may fail to stop the door, risking injury.

    Product
    CHRYSLER — CHRYSLER, DODGE TOWN AND COUNTRY, GRAND CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V086000·2012-03-05

    MCI Recalls 2012 Motor Coaches Due to Automatic Door Closing Hazard

    Motor Coach Industries is recalling 46 model year 2012 motor coaches because the entrance door may close without warning, increasing the risk of personal injury.

    Product
    MCI — MCI D4505, D4500, D4000ISTV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·11V477000·2011-09-16

    Vactor Jetter Sewer Cleaners Recalled for Safety Interlock Wiring Defect

    Vactor is recalling 2010-2011 Jetter-F and Jetter-V sewer cleaners because a safety interlock was incorrectly wired, allowing the vehicle to move while the operator is outside.

    Product
    VACTOR — VACTOR JETTER-V, JETTER-F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·10V055000·2010-02-23

    Honda Recalls 2005 Odyssey Touring for Power Liftgate Strut Defect

    Honda is recalling 21,776 model year 2005 Odyssey Touring vehicles because power liftgate gas struts may deteriorate early, causing the gate to close unexpectedly.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·09143·2009-03-05

    Rettig Belgium Recalls Wall-Mounted Radiators Due to Crush Hazard

    Rettig Belgium is recalling Radson wall-mounted radiators because they can fall from the wall, posing a crush hazard. One child's death was reported in Belgium.

    Product
    Radson Wall-Mounted Radiators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08611·2008-09-26

    Shivvers Recalls Lawn Mower Jacks Due to Collapse Hazard

    Shivvers Manufacturing is recalling about 450 lawn mower jacks because the lifting mechanism may fail, causing the mower to fall and potentially injure users.

    Product
    Jack Lift Tools and Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide